We assess the properties of deep neural network-reconstructed brain MR images in the high acceleration regime at factors up to 100. We have three contributions: 1) metrics on model performance from 2- to 100-fold accelerations, 2) a Monte Carlo procedure for scoring the quality of model reconstructions using only subsampled data, and 3) assessment of the acceleration effects on pathology in six cases. Our Monte Carlo procedure can estimate ground truth PSNR with coefficients of determination greater than 0.5 using only subsampled data. Our pathology results were stable in DNN reconstructions up to 8-fold acceleration.
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Figure 2: Diagram of Monte Carlo simulation pipeline. First, image phase and coil sensitivity maps are estimated from only the densely-sampled center region. Second, a simulated k-space is estimated by re-inserting phase into the DNN reconstruction, multiplying by sensitivity maps, applying the forward FFT, and adding noise. Multiple sampling patterns are applied and reconstructed. Monte Carlo metrics (SSIM or PSNR) are estimated using the original reconstruction as a ground truth.
Figure 3: Volume distortion metrics across accelerations, separated by contrast type. T1 images are the easiest to reconstruct (according to metrics). Observable are the two regimes: the standard reconstruction regime below an acceleration of 20 and the super-resolution regime above an acceleration of 20. Image quality declines rapidly as fewer peripheral k-space lines are sampled and the rate of decline is higher in the first regime.
Figure 4: Monte Carlo results across acceleration factors (A=Acceleration). MC estimates were obtained by running 5 iterations of the procedure in Figure 2, followed by estimating scaling and offset parameters. The results in this figure are shown on hold-out test data. MSE estimates were calculated via the MC PSNR estimate. We also show R2 scores for the estimates at each acceleration as an indicator of prediction quality. According to R2 values, the PSNR and MSE predictions have the highest fidelity. We aggregate R2 values for each metric to simplify presentation.
Figure 5: DL-based reconstructions in 3 illustrative cases (2 with pathology) at multiple undersampling schemes: (top) Normal healthy T2 image, (middle) T2-weighted pulse sequence in a patient with right frontal edema and mass effect, (bottom) T1-weighted post-contrast pulse sequence in a patient with a left heterogeneously enhancing, parieto-temporal lobe tumor. The quality of images with pathology decays considerably with the transition to the super-resolution regime. Four other pathology cases (not shown) had similar results.